Swedish Orphan Biovitrum AB (Publ)

Form 483

Stockholm, -, SwedenFEI 3003455777Issued May 04, 2018

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3003455777.

Observations1

Issue DateMay 04, 2018

StatusNo Warning Letter

Related Inspections7

Establishment Details

Firm: Swedish Orphan Biovitrum AB (Publ)
Location: Stockholm, -, Sweden
FEI Number: 3003455777
Product Type: Drugs
Issue Date: May 04, 2018
Country: Sweden

Inspection History, 2009 to 2019

NAI2

VAI5

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

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Swedish Orphan Biovitrum AB (Publ) FDA Form 483, Stockholm, May 4, 2018